Menu
GWAS Study

Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.

Tan MMX, Lawton MA, Jabbari E et al.

33111402 PubMed ID
GWAS Study Type
2848 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TM
Tan MMX
LM
Lawton MA
JE
Jabbari E
RR
Reynolds RH
IH
Iwaki H
BC
Blauwendraat C
KS
Kanavou S
PM
Pollard MI
HL
Hubbard L
MN
Malek N
GK
Grosset KA
MS
Marrinan SL
BN
Bajaj N
BR
Barker RA
BD
Burn DJ
BC
Bresner C
FT
Foltynie T
WN
Wood NW
WC
Williams-Gray CH
HJ
Hardy J
NM
Nalls MA
SA
Singleton AB
WN
Williams NM
BY
Ben-Shlomo Y
HM
Hu MTM
GD
Grosset DG
SM
Shoai M
MH
Morris HR
Chapter II

Abstract

Summary of the research findings

There are currently no treatments that stop or slow the progression of Parkinson's disease (PD). Case-control genome-wide association studies have identified variants associated with disease risk, but not progression. The objective of the current study was to identify genetic variants associated with PD progression.

2,848 individuals

Chapter III

Study Statistics

Key metrics and study information

2848
Total Participants
GWAS
Study Type
No
Replicated
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.